Abstract
In this work chemical derivatives of β-cyclodextrins (β-CD) have been considered and the inclusion constants with the racemic herbicide dichlorprop, only the (+) isomer of which being herbicidally active, have been determined. The experimental results showed that β-CD functional substituent affect both the inclusion constant values and the resolving power.
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© 1996 Springer Science+Business Media Dordrecht
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Trotta, F., Zerbinati, O., Giovannoli, C., Baggiani, C., Giraudi, G., Moraglio, G. (1996). Enantiomeric Separation of Dichlorprop by Capillary Electrophoresis Using β-Cyclodextrin Derivatives as Chiral Resolving Agents. In: Szejtli, J., Szente, L. (eds) Proceedings of the Eighth International Symposium on Cyclodextrins. Springer, Dordrecht. https://doi.org/10.1007/978-94-011-5448-2_141
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DOI: https://doi.org/10.1007/978-94-011-5448-2_141
Publisher Name: Springer, Dordrecht
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